Mitochondrial Damage-Associated Molecular Patterns: From Inflammatory Signaling to Human Diseases

被引:291
作者
Grazioli, Serge [1 ,2 ]
Pugin, Jerome [3 ]
机构
[1] Univ Geneva, Univ Hosp Geneva, Dept Pediat, Pediat Intens Care Unit, Geneva, Switzerland
[2] Univ Geneva, Dept Microbiol & Mol Med, Fac Med, Geneva, Switzerland
[3] Univ Geneva, Univ Hosp Geneva, Dept Anesthesiol, Intens Care Unit,Fac Med, Geneva, Switzerland
关键词
damage-associated molecular pattern; mitochondria; inflammation; pro-inflammatory cytokines; sterile inflammation; alarmins; FORMYL-PEPTIDE RECEPTORS; CA-2&-INDUCED MEMBRANE TRANSITION; SERUM CYTOCHROME-C; DNA COPY NUMBER; EXTRACELLULAR ADENOSINE-TRIPHOSPHATE; OBSTRUCTIVE PULMONARY-DISEASE; HOSPITAL CARDIAC-ARREST; INDEPENDENT ATP RELEASE; FIND-ME SIGNAL; DENDRITIC CELLS;
D O I
10.3389/fimmu.2018.00832
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Over the recent years, much has been unraveled about the pro-inflammatory properties of various mitochondrial molecules once they are leaving the mitochondrial compartment. On entering the cytoplasm or the extracellular space, mitochondrial DAMPs (also known as mitochondrial alarmins) can become pro-inflammatory and initiate innate and adaptive immune responses by activating cell surface and intracellular receptors. Current evidence indicates that uncontrolled and excessive release of mitochondrial DAMPs is associated with severity, has prognosis value in human diseases, and contributes to the dysregulated process observed in numerous inflammatory and autoimmune conditions, as well as in ischemic heart disease and cancer. Herein, we review that the expanding research field of mitochondrial DAMPs in innate immune responses and the current knowledge on the association between mitochondrial DAMPs and human diseases.
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页数:17
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